Canonical Allele Identifier: CA370394289

Gene: FGF20

Linked Data

• MyVariant Identifiers: chr8:g.16850648A>C (hg19) ; chr8:g.16993139A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16993139A>C , CM000670.2:g.16993139A>C	GRCh38
NC_000008.10:g.16850648A>C , CM000670.1:g.16850648A>C	GRCh37
NC_000008.9:g.16895019A>C	NCBI36
NG_015978.1:g.14027T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.569T>G MANE Select	ENSP00000180166.5:p.Phe190Cys
ENST00000180166.5:c.569T>G	ENSP00000180166.5:p.Phe190Cys
ENST00000519941.1:c.273T>G
NM_019851.2:c.569T>G	NP_062825.1:p.Phe190Cys
NM_019851.3:c.569T>G MANE Select	NP_062825.1:p.Phe190Cys